Benzyl Bromide → Benzyl 5-methyl-2-indolecarboxylate

HRID 844431

반응식

HRID 844431 반응식
[CH3:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[NH:7][C:6]([C:11]([OH:13])=[O:12])=[CH:5]2.C1CCN2C(=NCCC2)CC1.[CH2:25](Br)[C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1>CN(C=O)C>[CH3:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[NH:7][C:6]([C:11]([O:13][CH2:25][C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1)=[O:12])=[CH:5]2

참가 물질

5

반응물 3

HCID 7498Benzyl BromideHCID 811841,8-Diazabicyclo(5.4.0)undec-7-eneHCID 2591885-methyl-1H-indole-2-carboxylic acid

생성물 1

HCID 22612640Benzyl 5-methyl-2-indolecarboxylate

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

2.43 g of 5-methyl-2-indolecarboxylic acid are dissolved in 15 ml of DMF; 2.11 g of DBU are added and the mixture is then left stirring for 1 hour at RT. 2.61 g of benzyl bromide are added dropwise and the mixture is then left stirring for 6 hours at RT. This mixture is concentrated under vacuum and the residue is taken up in EtOAc, washed with water, with saturated Na2CO3 solution, with sulphate buffer and then with saturated aqueous NaCl. It is dried over Na2SO4 and then concentrated. The residue crystallizes from pentane and 3.3 g of the expected compound are obtained: m.p.=150-152° C.

후처리

  1. waitthe mixture is then left
  2. waitthe mixture is then left
  3. stirringstirring for 6 hours at RT
  4. concentrationThis mixture is concentrated under vacuum
  5. washwashed with water, with saturated Na2CO3 solution, with sulphate buffer
  6. dry with materialIt is dried over Na2SO4
  7. concentrationconcentrated
  8. customThe residue crystallizes from pentane and 3.3 g of the expected compound
  9. customare obtained

출처 및 근거

ORD 기록
ord-9b775c3404d04c898b6e568c3d3f402e
출처 데이터셋
uspto-grants-2002_04
특허 번호
US06380230B1

연결된 노트

불러오는 중…